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[3H]-monoamine uptake inhibition properties of kava pyrones.

作者信息

Seitz U, Schüle A, Gleitz J

机构信息

Institute of Naturheilkunde, University Clinics Ulm, Germany.

出版信息

Planta Med. 1997 Dec;63(6):548-9. doi: 10.1055/s-2006-957761.

Abstract

Three kava pyrones, the natural compounds (+)-methysticine and (+)-kavain, and the synthetic racemate (+/-)-kavain, were tested concerning their action on in vitro uptake of monoamines in synaptosomes prepared from the cerebral cortex and hippocampus of rats. (+/-)-Kavain and (+)-kavain were found to potently inhibit the uptake of [3H]-noradrenaline. Uptake of [3H]-noradrenaline was inhibited in the following order of potency: (+/-)-kavain = (+)-kavain > (+)-methysticine, whereas none of the kava pyrones efficiently blocked the uptake of [3H]-serotonin. The results indicate a pyrone-specific non-stereo-selective inhibition of the [3H]-noradrenaline uptake which might be responsible for or, at least, contribute to the psychotropic properties of kava pyrones.

摘要

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